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. 2014 Jun;52(6):2157-62.
doi: 10.1128/JCM.00691-14. Epub 2014 Apr 16.

Profiling of rpoB mutations and MICs for rifampin and rifabutin in Mycobacterium tuberculosis

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Profiling of rpoB mutations and MICs for rifampin and rifabutin in Mycobacterium tuberculosis

F B Jamieson et al. J Clin Microbiol. 2014 Jun.

Abstract

Resistance to rifampin (RIF) and rifabutin (RFB) in Mycobacterium tuberculosis is associated with mutations within an 81-bp region of the rpoB gene (RIF resistance-determining region [RRDR]). Previous studies have shown that certain mutations in this region are more likely to confer high levels of RIF resistance, while others may be found in phenotypically susceptible isolates. In this study, we sought to determine the relationship between the MICs of RIF and RFB and rpoB RRDR mutations in 32 multidrug-resistant (MDR), 4 RIF-monoresistant, and 5 susceptible M. tuberculosis clinical isolates. The MICs were determined using the MGIT 960 system. Mutations in the rpoB RRDR were determined by Sanger sequencing. RpoB proteins with mutations S531L (a change of S to L at position 531), S531W, H526Y, and H526D and the double mutation D516A-R529Q were associated with high MICs for RIF and RFB. Five isolates carrying the mutations L511P, H526L, H526N, and D516G-S522L were found to be susceptible to RIF. Several mutations were associated with resistance to RIF and susceptibility to RFB (F514FF, D516V, and S522L). Whole-genome sequencing of two MDR isolates without rpoB RRDR mutations revealed a mutation outside the RRDR (V146F; RIF MIC of 50 μg/ml). The implications of the polymorphisms identified in the second of these isolates in RIF resistance need to be further explored. Our study further establishes a correlation between the mutations and the MICs of RIF and, also, RFB in M. tuberculosis. Several rpoB mutations were identified in RIF- and RFB-susceptible isolates. The clinical significance of these findings requires further exploration. Until then, a combination of phenotypic and molecular testing is advisable for drug susceptibility testing.

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Figures

FIG 1
FIG 1
rpoB mutations and their correlation to RIF (A) and RFB (B) resistance levels. Asterisks indicate rpoB RDRR double mutants. Arbitrarily selected MIC ranges were used to catalogue resistance to RIF as high (MIC ≥100 μg/ml), medium (≥20 to <100 μg/ml), or low (≥1 to <20 μg/ml). Arbitrarily selected MIC ranges were used to catalogue resistance to RFB as high (MIC ≥5 μg/ml) or medium (≥0.5 to <5 μg/ml).

References

    1. World Health Organization. 2014. Global tuberculosis report 2013. World Health Organization, Geneva, Switzerland: www.who.int/tb/publications/global_report/en/
    1. Marsili L, Pasqualucci CR, Vigevani A, Gioia B, Schioppacassi G, Oronzo G. 1981. New rifamycins modified at positions 3 and 4. Synthesis, structure and biological evaluation. J. Antibiot. 34:1033–1038 - PubMed
    1. Ramaswamy S, Musser JM. 1998. Molecular genetic basis of antimicrobial agent resistance in Mycobacterium tuberculosis: 1998 update. Tuber. Lung Dis. 79:3–29. 10.1054/tuld.1998.0002 - DOI - PubMed
    1. Telenti A, Imboden P, Marchesi F, Lowrie D, Cole S, Colston MJ, Matter L, Schopfer K, Bodmer T. 1993. Detection of rifampicin-resistance mutations in Mycobacterium tuberculosis. Lancet 341:647–650. 10.1016/0140-6736(93)90417-F - DOI - PubMed
    1. Lee SS, Meintjes G, Kamarulzaman A, Leung CC. 2013. Management of tuberculosis and latent tuberculosis infection in human immunodeficiency virus-infected persons. Respirology 18:912–922. 10.1111/resp.12120 - DOI - PubMed

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